NDC 73027-207 Pronature Earth Conscious Hand Sanitizer With Aloe Vera Extract
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73027 - Jiangsu Hanhe Daily Chemicals Co., Ltd.
- 73027-207 - Pronature Earth Conscious Hand Sanitizer With Aloe Vera Extract
Product Packages
NDC Code 73027-207-01
Package Description: 60 mL in 1 BOTTLE
NDC Code 73027-207-02
Package Description: 300 mL in 1 BOTTLE
NDC Code 73027-207-03
Package Description: 500 mL in 1 BOTTLE
NDC Code 73027-207-04
Package Description: 30 mL in 1 BOTTLE
Product Details
What is NDC 73027-207?
What are the uses for Pronature Earth Conscious Hand Sanitizer With Aloe Vera Extract?
Which are Pronature Earth Conscious Hand Sanitizer With Aloe Vera Extract UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Pronature Earth Conscious Hand Sanitizer With Aloe Vera Extract Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CARBOMER 934 (UNII: Z135WT9208)
- TROLAMINE (UNII: 9O3K93S3TK)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Pronature Earth Conscious Hand Sanitizer With Aloe Vera Extract?
- RxCUI: 2287763 - ethanol 69 % Topical Gel
- RxCUI: 2287763 - ethanol 0.69 ML/ML Topical Gel
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".